Abnormal Uterine Bleeding Clinical Trial
Official title:
Effectiveness of Paracervical Block Versus Lidocaine Spray During Endometrial Biopsy Under Oral Analgesic Drugs; A Randomized Controlled Trial
Verified date | March 2014 |
Source | Mahidol University |
Contact | n/a |
Is FDA regulated | No |
Health authority | |
Study type | Interventional |
The purpose of this study to determine effectiveness of paracervical block, lidocaine spray and only oral analgesic drugs for pain relief during endometrial biopsy.
Status | Completed |
Enrollment | 120 |
Est. completion date | August 2014 |
Est. primary completion date | March 2014 |
Accepts healthy volunteers | Accepts Healthy Volunteers |
Gender | Female |
Age group | 30 Years to 70 Years |
Eligibility |
Inclusion Criteria: - abnormal uterine bleeding women - indicated for endometrial biopsy Exclusion Criteria: 1. contraindications to NSAID or Lidocaine - known sensitivity to these drugs 2. pregnancy 3. genital tract infection 4. coagulation disorder 5. unstable vital signs. |
Country | Name | City | State |
---|---|---|---|
Thailand | Akarawit Jitchanwichai | Songkla | Hatyai |
Lead Sponsor | Collaborator |
---|---|
Mahidol University |
Thailand,
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | Effectiveness of paracervical block VS Lidocaine spray during endometrial biopsy ; A randomized controlled trial | measurement outcome by record Pain score(NRS)[Numberical rating scale 0-10] immediately after procedure and 15 minutes after procedure in all groups Group 1(1%Lidocaine) Group 2(10%Lidocaine spray) Group 3 Control group(Placebo) Pain score immediately and Pain score 15 minutes were compared between group by using statistic analysis to indentify the significant of decreasing Pain score for pain relief during endometrial biopsy. And after that the result will used to determine effectiveness of each groups[ paracervical block, lidocaine spray and only oral analgesic drugs. |
up to 12 months | |
Secondary | adverse effects of paracervical block versus lidocaine spray | A secondary goal of this study was to determine the adverse effects of these methods(such as dizziness, nausea, vomiting, pelvic pain, bleeding) by recording the adverse effects outcome of each groups and report the result. | up to 12 months |
Status | Clinical Trial | Phase | |
---|---|---|---|
Recruiting |
NCT06067217 -
Comparative Study of Tranexamic Acid, Estrogen for Treatment AUB in DMPA Users
|
N/A | |
Completed |
NCT03638856 -
Comparing Effectiveness of Oral Misoprostal for Cervical Priming in Hysteroscopy
|
N/A | |
Recruiting |
NCT04172272 -
The Influence of TAP Block in the Control of Postoperative Pain After Laparotomy for Gynecological Procedures
|
N/A | |
Not yet recruiting |
NCT06050161 -
Evaluating Artisential Laparoscopic Instruments in Gynecologic Surgery
|
N/A | |
Completed |
NCT04381416 -
Study to Assess the Safety and Efficacy of the IUB SEAD™ Device
|
N/A | |
Recruiting |
NCT06193590 -
Suction Cervical Stabilizer Compared to Standard Tenaculum for Intrauterine Procedures
|
N/A | |
Completed |
NCT02192606 -
Does 3D Laparoscopy Improve Vaginal Cuff Suture Time?
|
N/A | |
Completed |
NCT03697733 -
Comparison Efficiency of Oral Etoricoxib Versus Intravenous Fentanyl on Post Operative Pain in Curettage Under TIVA
|
N/A | |
Completed |
NCT01721304 -
Decisionmaking for Abnormal Uterine Bleeding (AUB)
|
N/A | |
Completed |
NCT05406960 -
Therapeutic Effect of Herbal Infusion on Menometrorrhagia
|
N/A | |
Recruiting |
NCT06024109 -
Performance of SYMMCORA® vs. V-Loc® Suture Material in Patients Undergoing Laparoscopic Total Hysterectomy
|
||
Recruiting |
NCT06369012 -
Management of Abnormal Uterine Bleeding
|
N/A | |
Completed |
NCT06397898 -
NOVasure EXpierences (NOVEX)
|
N/A | |
Recruiting |
NCT05922657 -
A Registry to Gather Real World Use Data on the Cerene® Cryotherapy Device
|
||
Recruiting |
NCT04311073 -
Prophylactic Tranexamic Acid During Minimally Invasive Myomectomies
|
Phase 3 | |
Not yet recruiting |
NCT06398145 -
D-chiro-inositol and AUB
|
Phase 2 | |
Terminated |
NCT04475497 -
Role of Blood Management in Perioperative Outcomes
|
N/A | |
Recruiting |
NCT05062551 -
Effectiveness of Three Steps Hysteroscopic Repair of Post Caesarean Isthmocele in Patients With Post Menstrual Spotting
|
N/A | |
Terminated |
NCT05227456 -
Failed Endometrial Ablation Treatment With Implantable Progesterone (FEAT) Study
|
Phase 2 | |
Active, not recruiting |
NCT05299801 -
DAta MIning to Evaluate Novasure Treatment
|